Project Grant R01AI196563
- The National Institute of Allergy and Infectious Diseases (NIAID) awarded the University of Connecticut Health Center $263,375 on April 20, 2026 under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop antiviral therapies targeting herpes simplex virus alkaline nuclease. The funded research addresses drug-resistant HSV strains by identifying the HSV alkaline nuclease (encoded by the UL12 gene) as a novel target for antiviral drug discovery. Existing therapies rely on...
- The National Institute of Allergy and Infectious Diseases awarded Northwestern University $725,778 on August 19, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to investigate alphaherpesvirus axonal transport and neuroinvasion mechanisms. The research deciphers how neuroinvasive herpesviruses such as herpes simplex virus type 1 and pseudorabies virus invade the nervous system to establish lifelong latent infections; identifies intrinsic barriers to neural...
- The National Institute of Allergy and Infectious Diseases awarded Fred Hutchinson Cancer Center $465,116 on April 13, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop and evaluate AAV-delivered meganucleases as a therapeutic approach for durable control of genital herpes simplex virus infection. The R21 phase funds research extending prior work targeting HSV-1 to HSV-2, and determining whether intravenous or intrathecal administration is the optimal...
- The National Institute of Allergy and Infectious Diseases awarded the University of Pittsburgh $250,682 on February 19, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to investigate the role of nuclear paraspeckles in regulating herpes simplex virus type 1 (HSV-1) infection in neurons. The research examines how nuclear speckles and paraspeckles—subnuclear ribonucleoprotein structures involved in gene expression and RNA processing—modulate HSV-1 replication and...
- The National Institute of Allergy and Infectious Diseases awarded the University of Wisconsin–Madison $524,626 for a Project Grant (R01AI190006) on February 5, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855). The award funds research investigating how chromatin loops regulate the expression of anterograde transport genes during herpes simplex virus 1 (HSV-1) latency and reactivation. The research combines human neuronal platforms with chromosome conformation...
- The National Institute of Allergy and Infectious Diseases awarded Fred Hutchinson Cancer Center $238,899 on June 8, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to conduct preclinical evaluation of human monoclonal antibodies for herpes simplex virus type 2 (HSV-2) therapeutics. The research isolates and characterizes antibody-secreting cells discovered in genital skin tissue up to four months following HSV lesion healing. The project involves comprehensive...
- The National Institute of Allergy and Infectious Diseases awarded Albert Einstein College of Medicine $231,000 on June 1, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to identify, characterize, and develop human monoclonal antibodies whose primary protective mechanism is antibody-dependent cellular cytotoxicity (ADCC) for treatment and prevention of genital, neonatal, and recurrent herpes simplex virus (HSV) infections. The research builds on preclinical mouse...
- The National Institute of Allergy and Infectious Diseases awarded Temple University $237,751 on May 22, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop CRISPR-based attenuation of herpes simplex virus (HSV) as a strategy to improve immune control of genital herpes infection. The research leverages CRISPR-Cas9 technology to target the HSV UL56 gene, which encodes a viral protein that antagonizes innate immune sensing and affects virulence. Preliminary...
- The National Institute of Allergy and Infectious Diseases awarded The Regents of the University of Colorado, doing business as University of Colorado-Denver, $429,000 on June 9, 2026, for research investigating how extracellular vesicles released from varicella-zoster virus-infected neurons modulate herpes simplex virus type 1 neurovirulence. The project tests the hypothesis that non-infectious extracellular vesicles derived from VZV-infected neurons suppress innate immune responses in...
- The National Institute of Allergy and Infectious Diseases (NIAID), part of the Department of Health and Human Services National Institutes of Health, awarded $737,129 to Cleveland Clinic Lerner College of Medicine of Case Western Reserve University on August 13, 2026, for research on multifunctional peptide-based therapeutics for ocular diseases under the Allergy and Infectious Diseases Research program (CFDA 93.855). The project investigates keratin-derived antimicrobial peptides (KAMPs) as a...
The National Institute of Allergy and Infectious Diseases awarded the University of Illinois $796,976 on August 3, 2026, under the Allergy and Infectious Diseases Research program (CFDA 93.855) to develop a once-daily ocular nanoformulation of BX795, a non-nucleoside antiviral drug for herpes simplex virus keratitis therapy. HSV-1 keratitis causes corneal blindness globally, and current nucleoside antiherpetic treatments administered orally or topically prove insufficient, with emerging nucleoside-resistant strains driving demand for alternative therapeutics. BX795 inhibits hyperphosphorylation of eukaryotic translation initiation factor 4E-binding protein 1, constraining viral protein synthesis. Preliminary studies demonstrated that three-times-daily topical BX795 eyedrops significantly reduced infection in a mouse model, but the molecule's limited pH-dependent solubility and requirement for substantial dimethyl sulfoxide in solution necessitate formulation improvements to reduce dosing frequency and enhance ocular bioavailability. The research will convert BX795 into a hydrophobic salt using biocompatible anions, then transform the salt into a nanosuspension for once-daily long-acting topical therapy. Aim 1 focuses on developing various hydrophobic salts and characterizing the nanosuspensions for stability, in vitro antiviral activity, and ex vivo permeability. Aim 2 will evaluate long-term in vivo tolerability and in vivo antiviral efficacy of the lead BX795 hydrophobic salt nanosuspension formulation. Performance occurs in Chicago, Illinois. The award period runs through July 31, 2031. This is a Project Grant, the standard assistance type for NIH R01 research grants.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $797.0k | 7/30/26 |